Allele Registry

Canonical Allele Identifier: PA2825274487

Gene: EDA HGNC NCBI

ClinVar RCV:

RCV000414008

ClinVar Variation:

373096

HGVS (amino-acid)	Matching Registered Transcripts
NP_001005612.2:p.Tyr306Ser	CA16043303 NM_001005612.3:c.917A>C